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NCT00174798 · ClinicalTrials.gov registry record · Phase 2

MILADY: A Randomized, Placebo-controlled Safety and Efficacy Trial of SSR240600C in Treatment of Overactive Bladder or Urge Urinary Incontinence.

A Phase 2 study, sponsored by Sanofi.

Completed
Registry status
Phase 2
Development phase
118
Enrollment target

NCT00174798: Completed Phase 2 study, sponsored by Sanofi.

NCT00174798 is a Phase 2 study that has completed, run by Sanofi. The registered enrollment target is 118 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (11% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00174798, a Phase 2 study, has completed, sponsored by Sanofi.

COMPLETED
Registry status
Phase 2
Development phase
118 participants
Enrollment target

Study Summary

To evaluate the safety and efficacy of SSR240600C versus placebo on clinical and cystometric parameters in patients with OAB and UUI.

Interventions

  • DRUG Placebo
  • DRUG Tolterodine
  • DRUG SSR240600C

Trial Details

FieldValue
Enrollment Target 118 participants
Start Date 2005-05
Est. Completion 2006-05
Phase Phase 2
Sanofi

713 total trials

What the finished NCT00174798 record still lists

NCT00174798 is an interventional study that assigns participants to a tested intervention. The registered 118 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (11% lower).

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT00174798 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00174798 about?

NCT00174798 is a clinical study titled "MILADY: A Randomized, Placebo-controlled Safety and Efficacy Trial of SSR240600C in Treatment of Overactive Bladder or Urge Urinary Incontinence.". To evaluate the safety and efficacy of SSR240600C versus placebo on clinical and cystometric parameters in patients with OAB and UUI.

What is the current status of trial NCT00174798?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 118 participants. The study started on 2005-05. Estimated completion is 2006-05.

What interventions are being tested in trial NCT00174798?

The interventions under investigation include: Placebo (DRUG), Tolterodine (DRUG), SSR240600C (DRUG).

Who is sponsoring clinical trial NCT00174798?

This trial is sponsored by Sanofi, which has 713 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00174798's enrollment target sits among peer trials

118 618th of 2000 higher than 1,378 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00174798, the US trial registry maintained by the National Library of Medicine. NCT00174798 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.